| Literature DB >> 18489063 |
Nicholas K Brown1, Daniel J McCormick, Vladimir Brusic, Chella S David, Yi-Chi M Kong.
Abstract
The A-E+ transgenic mouse is highly susceptible to human thyroglobulin (hTg)-induced thyroiditis, but strongly tolerant to a challenge by mouse thyroglobulin (mTg), in stark contrast to traditionally susceptible strains, wherein mTg induces stronger thyroiditis. To identify mouse thyroid epitopes recognized by destructive, hTg-primed T cells, we selected the three hTg epitopes known to be presented by H2E(b), as the basis for synthesizing potential mTg epitopes. One 15-mer peptide, mTg409, did prime T cells, elicit Ab, and induce thyroiditis. Moreover, cells primed with corresponding, pathogenic hTg410 cross-reacted with mTg409, and vice versa. mTg409 contained 4/4 anchor residues, similar to the corresponding hTg peptide. Based on this finding, a second mTg epitope, mTg179, was subsequently identified. These mTg autoepitopes, identified by using thyroiditogenic hTg epitopes, help to explain the severe thyroiditis seen in this novel A-E+ transgenic model.Entities:
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Year: 2008 PMID: 18489063 PMCID: PMC2483956 DOI: 10.1016/j.cellimm.2008.02.002
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868